A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17101376



Internal ID21476716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:6316017..6316017hg38UCSC Ensembl
chr18:6316016..6316016hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5657277
Supporting Variants
SamplesHG03486
Known GenesL3MBTL4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17101376
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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